Finlandssvenska åsikter om och attityder till modern språkpåverkan

The study describes and analyzes Finland Swedes attitudes to modern-day linguistic influence, the relationship between informants explicitly reported views and the implicit attitudes they express towards language influence. The methods are primarily sociolinguistic. For the analysis of opinions and attitudes I have further developed and tested a new tool in attitude research. With statistical correlation analysis of data collected through a quantitative survey I describe the views that Swedish-language Finns (N=500) report on the influence of English, on imports, and on domain loss. With experimental matchedguise techniques, I study Finland-Swedes (N=600) subconscious reactions to English imports in spoken text. My results show that the subconscious reactions in some respects differ markedly from the views informants explicitly report that they have: informants respond that they would like English words that come into Swedish to be replaced by Swedish replacement words, but in a matched-guise test on their subconscious attitudes, the informants consider English words in a Swedish context to have a positive effect. The topic is further dealt with in interviews where I examine 36 informants implicit attitudes through interactional sociolinguistic analyses. This study comes close to pragmatic discourse analysis in its focus on pragmatic particles and modality. The study makes a rather strict distinction between explicitly expressed opinions and implicit, subconscious attitudes. The quantitative analyses suggest that the opinions we express can be tied to the explicit in language. The outcome of the matched-guise test shows that it is furthermore possible to find subconscious, implicit attitudes that people in actual situations rely on when they make decisions. The discourse analysis finds many subconscious signals, but it also shows that the signals arise in interaction with one s interlocutor, the situation, and the norms in the society. To account for this I have introduced the concept of socioconscious attitude. Socioconscious attitudes reflect not only the traditions and values the utterer grew up with, but also the speaker s relation to the social situation (s)he takes part in.

Det grekiska dramat. En Studie av euroländeras agerande i Greklandskrisen.

Jag granskar i min avhandling pro gradu den ekonomiska krisen i Grekland som kulminerade under vären 2010 när Grekland vände sig tili de övriga medlemsländerna i Ekonomiska och monetära Unionen (EMU) med en förfrägan om ekonomisk hjälp i formav län. Syftet med avhandlingen är att undersöka hur de övriga EMU-medlemmarna fattade sitt beslut om att ekonomiskt stöda Grekland efter att landets kreditvärdighet sänkts av de internationella kreditvärderingsinstituten. Jag granskar Greklandskrisen och dess utveckling, de lösningar som man gick in för inom ramen för valutaunionen, hur besluten om stödpaketet fattades och vilka faktorer som päverkade besluten. Jag tar avstamp i Optimum Currency Area-teorin (OCA-teorin) och teorier om europeisk ekonomisk integration. Dessutom för jag en diskussion kring solidariteten mellan EUländerna, som ocksä använts som argument för stödpaketet tili Grekland. Jag klassificerar euroländerna utgäende för hur det nationella beslutet om Greklandspaketet fattats och gör därefter en agglomerativ klusteranalys, med ambitionen att förklara vilka faktorer som päverkat besluten. Syftet med klusteranalysen är att klargöra huruvida politiska faktorer, som härrör sig tili regeringen och dess sammansättning, eller ekonomiska faktorer, som bclyser statsfinansernas tillständ, bäst förklarar hur ett land fattat sitt beslut. Resultatet visar att de politiska variablerna har päverkat ländernas beslut mer an de ekonomiska, men förklaringsgraden är relativt lag i bägge fallen. Jag för vidare en diskussion om resultatet ur ett OCA-perspektiv, kriterierna för ett optimalt valutaomräde samt EMU:s utveckling i dito riktning. Jag avslutar avhandlingen med en diskussion kring EMU:s framtid.

Molecular diagnosis of developmental disorders

ABSTRACT Idiopathic developmental disorders (DDs) affect ~1% of the population worldwide. This being a considerable amount, efforts are being made to elucidate the disease mechanisms. One or several genetic factors cause 30-40% of DDs, and only 10% are caused by environmental factors. The remaining 50% of DD patients go undiagnosed, mostly due to a lack of diagnostic techniques. The cause in most undiagnosed cases is though to be a genetic factor or a combination of genetic and environmental factors. Despite the surge of new technologies entering the market, their implementation into diagnostic laboratories is hampered by costs, lack of information about the expected diagnostic yield, and the wide range of selection. This study evaluates new microarray methods in diagnosing idiopathic DDs, providing information about their added diagnostic value. Study I analysed 150 patients by array comparative genomic hybridization (array CGH, 44K and 244K), with a subsequent 18% diagnostic yield. These results are supported by other studies, indicating an enourmous added diagnostic value of array CGH, compared with conventional cytogenetic analysis. Nevertheless, 80% of the patients remained undiagnosed in Study I. In an effort to diagnose more patients, in Study IV the resolution was increased from 8.9 Kb of the 244K CGH array to 0.7 Kb, by using a single-nucleotide polymorphism (SNP) array. However, no additional pathogenic changes were detected in the 35 patients assessed, and thus, for diagnostic purposes, an array platform with ca 9 Kb resolution appears adequate. The recent vast increase in reports of detected aberrations and associated phenotypes has enabled characterization of several new syndromes first based on a common aberration and thereafter by delineation of common clinical characteristics. In Study II, a familial deletion at 9q22.2q22.32 with variable penetrance was described. Despite several reports of aberrations in the adjacent area at 9q associated with Gorlin syndrome, the patients in this family had a unique phenotype and did not present with the syndrome. In Study III, a familial duplication of chromosome 6p22.2 was described. The duplication caused increased expression of an important enzyme of the γ-aminobutyric acid (GABA) degradation pathway, causing oxidative stress of the brain, and thus, very likely, the mild mental retardation of these patients. These two case studies attempted to pinpoint candidate genes and to resolve the pathogenic mechanism causing the clinical characteristics of the patients. Presenting rare genetic and clinical findings to the international science and medical community enables interpretation of similar findings in other patients. The added value of molecular karyotyping in patients with idiopathic DD is evident. As a first line of testing, arrays with a median resolution of at least 9 Kb should be considered and further characterization of detected aberrations undertaken when possible. Diagnostic whole-exome sequencing may be the best option for patients who remain undiagnosed after high-resolution array analysis.